Wieraszko A
CSI/IBR Center for Developmental Neuroscience and Developmental Disabilities, College of Staten Island, City University of New York 10314.
J Neurochem. 1995 Mar;64(3):1097-101. doi: 10.1046/j.1471-4159.1995.64031097.x.
The influence of suramin, a suggested purino-receptor antagonist, on the evoked synaptic potentials recorded from hippocampal slices was evaluated. The suramin induced a nondecremental, concentration-dependent amplification of the slope of excitatory postsynaptic potential and magnitude of the population spike (long-term potentiation, LTP). The effect of suramin was completely abolished by adenylimidodiphosphate, a non-hydrolyzable analogue of ATP, and markedly reduced by NMDA-receptor antagonists DL-2-amino-5-phosphonovaleric acid and MK-801. These results indicate that, in addition to acting as an antagonist of P2 receptors, suramin is also able to facilitate hippocampal potentials in a way that involves mechanisms participating in induction of LTP.
对一种被认为是嘌呤受体拮抗剂的苏拉明,评估其对海马切片记录的诱发突触电位的影响。苏拉明诱导兴奋性突触后电位斜率和群体峰电位幅度呈非递减的、浓度依赖性放大(长时程增强,LTP)。ATP的非水解类似物腺苷亚胺二磷酸可完全消除苏拉明的作用,而NMDA受体拮抗剂DL-2-氨基-5-磷酸戊酸和MK-801可显著降低其作用。这些结果表明,除了作为P2受体的拮抗剂外,苏拉明还能够以涉及参与LTP诱导机制的方式促进海马电位。